Misu Y, Kuwahara M, Kaiho M, Kubo T
Eur J Pharmacol. 1983 Jul 22;91(2-3):287-90. doi: 10.1016/0014-2999(83)90480-6.
Presynaptic beta-adrenoceptors were further characterized in spiral strips of guinea-pig pulmonary arteries preloaded with [3H]norepinephrine. l-Metoprolol (3 X 10(-6) M) inhibited isoproterenol (3 X 10(-7) M)-induced increases in 3H efflux by transmural field stimulation, whereas the d-isomer produced no inhibition. However, IPS 339, H 35/25, butoxamine and metoprolol (3 X 10(-6) M) antagonized salbutamol (3 X 10(-7) M)-induced increases in the parameter, whereas acebutolol, bevantolol and practolol (3 X 10(-6) M) produced no antagonism. Presynaptic beta-adrenoceptors in guinea-pig pulmonary arteries appear to have characteristics similar to those postsynaptic classical beta-adrenoceptors.
在预先用[3H]去甲肾上腺素加载的豚鼠肺动脉螺旋条中,对突触前β-肾上腺素能受体进行了进一步的特性研究。左旋美托洛尔(3×10⁻⁶ M)可抑制异丙肾上腺素(3×10⁻⁷ M)通过跨壁场刺激诱导的3H外流增加,而右旋异构体则无抑制作用。然而,IPS 339、H 35/25、布托沙明和美托洛尔(3×10⁻⁶ M)可拮抗沙丁胺醇(3×10⁻⁷ M)诱导的该参数增加,而醋丁洛尔、贝凡洛尔和普拉洛尔(3×10⁻⁶ M)则无拮抗作用。豚鼠肺动脉中的突触前β-肾上腺素能受体似乎具有与突触后经典β-肾上腺素能受体相似的特性。